Director Quality Assurance Operations

Job Description

For our Animal Health location in Boxmeer, we are currently recruiting a Director Quality Assurance Operations.

Welcome to our team

Our production facilities in Boxmeer are part of our global animal health production network and manufacture and package animal health products according to Good Manufacturing Practices (GMP) standards. Our production organization consists of several Integrated Process Teams (IPTs) and Centers of Excellence (CoEs). Our Quality Assurance group, with approximately 150 employees, ensures every single material used inside our products is purchased, manufactured, processed, tested, packaged, stored, and distributed in alignment with our high standards of quality and all regulatory requirements. To guide this group through a dynamic phase of growth, innovation, and expansion, we are looking for a Director Quality Assurance Operations.

About the role

Reporting into our Boxmeer Site Quality Lead, and as part of the Site Quality Management Team, you are responsible for translating global, regional, and site quality priorities into a clear operational strategy that ensures compliant, uninterrupted supply of vaccines and pharmaceuticals. Beyond day-to-day QA leadership, the role shapes the long-term direction of QA operations by strengthening batch release flow, building robust cross-site handoffs, improving decision-making through KPIs and metrics, and driving continuous improvement and digitization across site quality processes. The role acts as a key strategic interface between QA, QC, manufacturing, and global quality teams, ensuring that quality systems, standards, and governance are aligned, scalable, and future-ready. It also owns the development of the QA organization, building a capable and agile team while embedding operational excellence, compliance, and performance management into the function.

Tasks and responsibilities

• Lead and develop the Quality Assurance Operations team (5 direct reports, approximately 100 employees).
• Translate Quality organization strategy into QA Operations plans.
• Design, plan, and implement the operational QA strategy in line with global, regional, and site quality goals.
• Manage QA Operations budget and required reporting.
• Shape, implement, and continuously improve strategic plans for QA Operations.
• Oversee batch release processes and end-to-end batch tracking.
• Monitor KPIs, use metrics for decision-making, and take corrective actions when needed.
• Identify business trends through metrics and adjust actions accordingly.
• Initiate, prioritize, manage, and coordinate improvement initiatives for QA Operations in collaboration with other site functions.
• Develop, implement, and maintain standards, procedures, and guidelines within the Manufacturing Division, especially in review and release areas.
• Ensure QA Operations processes comply with relevant regulations and requirements.
• Solve problems, escalate issues appropriately to global teams, and keep relevant stakeholders informed.
• Determine the QA Operations project portfolio in alignment with partner IPTs.
• Lead and/or participate in site projects and provide quality oversight and support.
• Develop a strategy for smooth batch flow, including multi-site product releases.
• Build robust inter-site processes, clear communication flows, and defined handoffs between sites and functions.
• Work closely with global quality management, health authorities, and site operations management.

Your profile

• Academic degree in a relevant field such as Pharmacy, Medical Biology, (Bio)Chemistry, (Bio)Process Technology, or related scientific disciplines, combined with at least 7–10 years of relevant experience in an international pharmaceutical company.
• Proven track record of managing and developing large organizations and leading other managers in a complex and relevant organization.
• Strong leadership capabilities, with the ability to inspire, develop, and align diverse teams across regions and functions.
• Demonstrated success in stakeholder management, building trusted partnerships and influencing effectively across organizational levels.
• Solid understanding of GMP, cGMP compliance, quality systems, and relevant manufacturing regulations.
• Experience working with health authorities and managing audits and inspections.
• Excellent command of the English language, both oral and written.

What we offer

You will join an organization at a pivotal moment of growth, with increasing demand for both existing and new products and a strong focus on innovation and expansion.

• Competitive compensation aligned with your knowledge and experience.
• 3% year-end payment and an annual bonus based on individual and company performance.
• Company car or car allowance.
• A minimum of 25 days of leave.
• Solid pension plan.
• Excellent accessibility: the train station is right by our main entrance and there is ample parking.
• High-quality company restaurant with fresh, healthy options daily.
• Contribution toward your personal sports/fitness membership to support your vitality.
• Beautiful private park on the premises, ideal for a walk, break, or moment of relaxation.
• Mental well-being support via Lyra Health for you and your family members.
• Access to a dedicated prayer/meditation room.

Animal Health

Our Animal Health Division is a trusted global leader in veterinary medicine, dedicated to preserving and improving the health, well-being, and performance of animals and the people who care for them.

Required Skills

cGMP Compliance, Change Management, Decision Making, Driving Continuous Improvement, GMP Compliance, New Product Development, Operational Excellence, Operations Management, People Leadership, Quality Assurance (QA), Quality Management Systems (QMS), Stakeholder Management, Strategic Planning